Specifications

Section 2
Introduction
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Research Instruments Ltd
2
SECTION 2 - INTRODUCTION TO RI WITNESS
Indication for Use for RI Witness System
To identify and track human samples, using RFID technology, through the assisted reproduction
(AR) cycle, including cryopreservation.
Contraindication:
This device is not intended to be exposed to known sources of electromagnetic interference
(EMI) with medical devices such as diathermy, CT, MRI, RFID (except other RI Witness RFID
components) and electromagnetic security systems, e.g. metal detectors and electronic article
surveillance systems.
Applicable indications for use are subject to the regulations of the country into which the device
is sold. Availability of RI Witness for clinical use is dependent on the regulatory approval status
of RI Witness within the country the device is intended to be sold into.
Applicable Part Numbers
Related Documents
6-70-121UM RI Witness WorkArea Software Manual
6-70-122UM RI Witness Manager Software Manual
Compatibility
RI Witness is used in conjunction with the following:
• Essential medical devices, e.g. dishes and tubes, maybe AR or non-AR specic.
• Non-essential medical devices, e.g. safety cabinets, incubators, micromanipulators, lasers.
• Non medical devices (general laboratory equipment), e.g. work benches, microscopes, PCs.
This device has RFID reader capability. If it is the intention that it be employed in a clinical lab, we
recommend its use alongside other medical devices and that the performance of these medical
devices be monitored for potential eects of EMI disturbances, and reported when appropriate.
Installation
Installations of the RI Witness Sperm Preparation Reader should be carried out by a RI technician
or other RI authorised personnel. Incorrect installation could result in overall poor performance.
Part Number Descripon
6-70-854 RI Witness Sperm Preparation Reader